Canonical Allele Identifier: PA105734
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 30185

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005682.2:p.Thr1547Ile
CA129007
NM_005691.3:c.4640C>T